signet 615 anaesthesia workstation signet 615 anaesthesia
Contents
1. VisiWink Supply Pressure Indicator Scavenge Connector Block Oxygen Connector Medical Gas Flowmeters Selectatec Vaporiser Mounting Medical Gas Flow Controls 2 1 Gas controls The ON OFF switch is mounted on the top right hand side and when activated allows for the supply of gases to be made available for use The ON OFF switch also turns on the flowmeter backlight On the left hand side of the control console are the gas flow controls and rotameters Gas controls can be differentiated by their shape and colour The white oxygen 02 control is furthest to the left and to international design standards The nitrous oxide N20 control is dark blue and air is black The basic Signet 615 is a three gas five tube machine with two tubes each for nitrous oxide and oxygen It can also be supplied with only two tubes nitrous oxide and oxygen 2 2 Flowmeters Having passed through the system each gas enters the base of the anti hypoxic device via the flow control valve into flowmeter The flow control valves allow for fine adjustment of the flow rate through each of the flowmeter tubes rotameters This ensures that accurate gas mixtures are achieved 10 Signet 615 User Manual When the flow control valve s is are opened the gas continues at low pressure upward through the flowmeter tube whose float responds to indicate the rate of flow in litres per minute or parts thereof Note that the rat2. 26 Signet 615 User Manual exceeds the applicable RF compliance level above the anaesthetic workstation should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as reorienting or relocating the anaesthetic workstation 7 2 4 Recommended Separation Distances from Portable and Mobile RF Communication Equipment The anaesthetic workstation is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The user of the anaesthetic workstation can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the anaesthetic workstation as recommended below according to the maximum output power of the communications equipment Rated maximum Separation distance according to frequency of transmitter output power of m transmitter 150 kHz to 80 MHz 80 MHz to 800 800 MHz to 2 5 GHz Ww d 1 2VP MHz d 2 3VP d 1 2VP 0 01 0 1 0 1 0 2 0 1 0 4 0 4 0 7 1 1 3 1 3 2 3 10 3 8 3 8 7 3 100 12 0 12 0 23 0 Notes e At 80 MHz and 800 MHz the separation distance for the higher frequency range applies e These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people For transmitters rated at a maximum output
3. ulco medical SIGNET 615 ANAESTHESIA WORKSTATION USER MANUAL Signet 615 User Manual Copyright 2002 2005 by Ulco Medical All rights reserved No part of this publication may be reproduced in any form in an electronic retrieval system or otherwise without the written permission of the Ulco Medical All Ulco products are subject to a program of continuous development and the manufacturer reserves the right to make alterations in design and equipment without prior notice Document Number SG6 UM 001 Version 1 2 CE Signet 615 User Manual Table of Contents 1 Introduction s sssssnnsnnnnnnunnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnn nnmnnn nnmnnn 6 Teh Warranty Statement s sess ennen benini Nanke NERE KENEK EUAS Nakai 6 12 Abo t this man als sesei penan aiian nes eae Oaea 6 1 3 WARGO GOS Gas enccendienssandieenttadinnsegndaenniged a a aa E E 6 1 4 Device Classification cccccccccceeeeeseeeecceeeeeeeeeeseeeeeeeeeeeeeeeeeseeenaeeeeeeeeeeeeeeee 7 1 5 Background ssmeiicssiiniriserda irian daiide aiaa daad enda d aaia adiada 7 1 6 Major features icsicescecctescivesteasepsctnastnasisasesanteacnessinasioncuaecivacinasiessttecusecieaninagiodec 7 1 6 1 Overall strengths eee cece eee ceeeeeceeeeeeeeeeeseeacaeeeeeeeeeeeeeseseneeeeeeeeeees 7 1 6 2 Typical configuration x 0 2c scccssnseneisascsnnnedsoanniiy ie eoadaeedeahannnaaseeasioondnneds 7 1 7 Safety PI6
4. Emissions test Compliance Avoiding Electromagnetic Interference Radio Frequency Group 1 The anaesthetic workstation uses RF energy only for its RF emissions internal function Therefore its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment RF emissions Class A The anaesthetic workstation is suitable for use in all CISPR 11 Harmonic emissions IEC 61000 3 2 Voltage fluctuations IEC 61000 3 3 establishments other than domestic and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes Not applicable Not applicable 7 2 2 Electromagnetic Immunity The Signet 615 anaesthetic workstation is suitable for use in the specified electromagnetic environment The user must ensure that it is used in the appropriate environment as listed below Immunity test IEC60601 test level Compliance level Electromagnetic environment guidance Electrostatic discharge ESD IEC61000 4 2 6 kV contact 8kV air Floors should be wood concrete or ceramic tile If floors are covered with synthetic material the relative humidity should be at least 30 Electrical fast transient burst 2 kV for power supply lines Mains power quality should be that of a typical commercial or hospital environment IEC 61000 4 4 1 kV for input output lines Surge 1 kV differential mod
5. See the user manual for the particular accessory in order to determine how it should be disinfected The workstation will require disinfection only if the exterior surfaces become directly contaminated disinfection in such cases is described in Section 5 2 WARNING Always disconnect the workstation from the mains supply prior to carrying out maintenance and cleaning 5 1 Cleaning The machine must be disconnected from the mains before cleaning or disinfecting The workstation s outer surfaces can be cleaned using a soft cloth and mild soap solution such as Lemex Clean the following surfaces Frame uprights and side panels Plastic surfaces skirt front panel top Metal work table Absorber mounting posts and side rails Do not use ammonia phenol or acetone based cleaners After washing wipe with clean water and allow to dry Do not allow fluids to penetrate the housing or any of the external connectors 5 2 Disinfecting Anaesthetic workstations need not be disinfected unless directly contaminated If the equipment has become contaminated and the affected part is removable it may be cleaned using a washer Meile or similar Chemical disinfecting e Wash with a soft cloth and soap solution and then dry e Wipe again with 2 glutaraldehyde pH 6 5 solution e Allow to stand for 20 minutes e Rinse and dry thoroughly 3 Steam Autoclaving Normally this is not required for anaesthesia equipment and accessories
6. Signet 615 User Manual 7 2 3 Recommended Separation Distance 7 2 4 Recommended Separation Distances from Portable and Mobile RF Communication Equipment ccccceeeeeeeeeeeeeeneeeeeeeeeeeeeeeceneeeeeeeeeeeeeeeee 27 Ta SYMPOSIA eE AE 27 Te Standard WOM aaa Ea a E a aa Ea 28 7 Optional Mern Sedici edida eed diriana ndaid enanada daia daada adidasa 28 Terms and conditions sis cssasscasecessastacireasacessececcanvecesnceceacaaesdnasseanes 29 Signet 615 User Manual 1 Introduction 1 Warranty Statement All Ulco products are guaranteed to be free of defects of workmanship or material for a period of one year from the date of delivery The following are exceptions to this warranty 1 Defects caused by misuse mishandling tampering or by modifications not authorised by Ulco or its appointed agents are not covered N Rubber and plastic components and materials are warranted to be free of defects at the time of delivery Any product which proves to be defective in workmanship or material will be replaced credited or repaired with Ulco holding the option Ulco is not responsible for deterioration wear or abuse In any case Ulco will not be liable beyond the original selling price Goods are subject to the terms of applicable warranty Defective products will be accepted for return at Ulco s discretion and only during the warranty period Application of this warranty is subject to the following co
7. they should only be used with equipment supplied by Ulco in order to ensure compliance with the relevant electrical safety standards IEC 60601 1 1 One external IEC outlet is mounted in the side strip of the machine for use in powering vaporisers The Signet has been safety tested in conjunction with TEC 4 Desflurane vaporisers only If a more flexible external outlet solution is required the APB7O see Section 2 18 1 may be purchased as an option but system testing to the safety standard will become the responsibility of the purchaser Signet 615 User Manual 2 18 Other accessories Suction apparatus A mounting exists which accepts a special swivel bracket that supports the suction receivers from Abbott or other similar brands The bracket is an optional item and can be ordered direct from Ulco as P N ASU203 Another accessory which can be supplied on the side is a fold down writing tray This is attached by a simple quick locking mounting block on the rail on the side of the work area The tray can be secured in a horizontal position by swinging the arm brace out from under the tray Many other accessories can be mounted on the rail via this method for example a universal circuit support arm able to swivel in many directions The lock screw on the side can control excessive movement Hooks are mounted to the bottom back panel and a movable sphygmomanometer mount is positioned on the top monitor tray An aneroid or mercuri
8. 15 Patient circuitry ULCO manufactures many different types of patient circuitry All are connected to the fresh gas line from the common gas outlet The first circuit is the Magill s circuit or Mapleson A It is a spontaneous breathing circuit and is supplied with a mask The exhaust valve is fitted with a scavenging connector The second circuit is a Bain or Mapleson D or E Again a scavenging connector is fitted The third circuit is the paediatric circuit which goes by many names and comes in many different configurations from many manufacturers It is suitable for small children and neonates and comes supplied with three masks The circle circuit however is the most common option 2 15 1 The circle circuit For this the absorber is connected to the common gas outlet Ulco supplies absorbers in a 1 or 2kg model with an integrated manual bag vent switch Part No AB800 This absorber has separate limbs for the ventilator and manual bag selection of the limb connected to the circle circuit is made by switching a rotary knob either to the bag or ventilator position This eliminates the need to remove the manual bag from the single limb to attach it to the ventilator The absorber can be fitted with an optional Manometer gauge Part No AB 400 2 16 Oxygen failure warning device This is a nitrous oxide cut off and whistle alarm In the event of a complete loss of oxygen from both the wall gas and cylinder gas supply the machine and t
9. should be checked according to specified protocols Attention should be given to 2 2 6 1 Equipment used for airway maintenance and intubation of the trachea 2 2 6 2 Suction apparatus 2 2 6 3 Gas analysis devices 2 2 6 4 Monitoring equipment Special attention should be paid to alarm limits and any necessary calibration 2 2 6 5 Intravenous infusion devices 2 2 6 6 Devices to reduce hypothermia during anaesthesia 2 2 6 7 Breathing circuit humidifiers 2 2 6 8 Breathing circuit filters 2 2 7 Final check Ensure vaporisers are turned off and that the breathing system is purged with air or oxygen as appropriate Level three check Immediately before commencement of each anaesthetic the anaesthetist should 2 3 1 Check a changed vaporiser using the protocol outlined in 2 2 2 2 2 3 2 Check a changed breathing circuit using the protocol outlined in 2 2 2 4 2 3 3 Check that equipment as specified in 2 2 6 is ready for the next case 18 Signet 615 User Manual This policy document has been prepared having regard to general circumstances and it is the responsibility of the practitioner to have express regard to the particular circumstances of each case and the application of this policy document in each case Policy documents are reviewed from time to time and it is the responsibility of he practitioner to ensure that the practitioner has obtained the current version Policy documents have been prepared having reg
10. 3 2 2 General preparation pre ChECK ceeeeeeeseceeeeeeeeeeeseeneeeeeeeeeeeeees 20 e223 CCylinder FNO eet sehen con neces se cee cece aa a aar hE bara 20 3 2 4 Component integrity 28st cccudvewenteSesuonceletaenvelesessoedvtwcute Uevuvaueleencesuleels 20 oes AON K el teed t sats Maat ct sada ta cc ada eo nde alls A 20 OD Gr ANON T TTE 21 4 1 Medical Gas MMO ts siinc terete Mathes diate ein ei eine erent 21 4 1 1 Accuracy and the Effects of BackpreSSure ccceeeeeeeeeeeeeeeeeeeees 21 4 2 RICO OY SIG INS a aa aana iaaa Vata ed vad a iae 21 4 3 Troubleshooting ke ae ih he a a eh eee ea ar ca ere eae eae eae ce a 21 ASel WLCAKS cxattsctatatemteeietate acter EE T 21 Gare and Cleaning srn naaa naaar aaa seas ace ne cee rC Uaine ea etedeaceee 23 Sell ClGANING accessor aa aA E EEA E AA 23 52 DisinfectiNg sheen annn a es tetoeee ae 23 53 Steam AUIOCIAVING 22 an ite tar tees Si ha eee cde A a 23 S4 RIETS ea aia CBSE Red eee Pay CBSE Red set Ray E aee Ruy ebesaes 23 DENVICING a so essere seat eee ce eee reac eee a cassette 24 6 1 Service intervals and service components for Signet 615 24 Specifi A ON S u a occa eee See ae 25 TA PAYSA a ciel oe hee hte E E ae he E AER 25 7 2 Electromagnetic Compatibility cccceceeeeeeceeeeneeeeeeeeeeeeeeeenneeeeeeeeeeeeeeeaes 25 7 2 1 Electromagnetic Emissions incur raed ae dea iad 25 7 2 2 Electromagnetic Immunity ticoxces acces cones ios corene nan weacoee ante 25
11. CaMONSsiccnacarniciarnimmtacnusincciacatnumtacvetadmuatancnnsncniwedians 8 1 7 1 Powering the unit up for the first time ccecccceeeeeeeeeeeeeseeeeeeeeeees 8 1 7 2 Follow the Instructions for USC cccceceeeeeeeeeeeeeeeeeeeeeeeeeeeeneeneeeeeeeees 8 1 7 3 Liability for proper function or damage ccceeeeeeeeeeeeeeteeeeeeeeees 8 1 7 4 Maintenance and Repairs cccceeceeeeeeeeeeeeeeeneeeeeeeeeeeeeeeeeneneeeeeeeees 8 1 7 5 Use of anaesthetic agents ccccccceeeeeeeeeeeeeeeceeeeeeeeeeeeeenaeeeeeeeeeeeees 8 1 7 6 Power CONGO WOM isst snaise aina a ai hs 8 1 7 7 Monitoring and alarmS seeeseseeeneeeeeeeerrrrrrrreserrenrrrnrnrsserrrrrrnnneneeeene 9 2 Major components of the machine ssssssssnnnnnnnnnnnnnnnnnnnnnnnnnn nnne 10 2 1 Gas c ntrolS eerecssi nea a EN ee ee ee a eee 10 2 2 FIOWMEtOIS oee e errr reer omer rer E E er 10 2 3 Patent BlOCK sssiskoi pecs seeecte srin noii rraren soba naranai inania nieee i aab nanii ian 11 2 4 NAD ONS ONG oie ct cntectncitaeccearteaiecinch tread aadumndnaictnnndaanduencnnitemnanastneuincuunedeentaaneincs 11 MON AUON wcscsctcc sc sencedigdencetios Resi ndthesSieaitiebieiDnad tas osescitnahNectieses cibbestiaSiadeis 12 2 6 Soda lime ADSOM Sl ns 5 sie cccenciennsansinencaadiannstesinnniandsannsdaptvantaabianncdedieecisadianuids 12 2 7 The anti hypoxic device ceeic sceceiss since tecetecedesuieeeaianieceieniie miauieenieeuiaeeseanbaeuine 12 28 G
12. There are no components of the Signet workstation which can be autoclaved 5 4 Filters Always fit a new single use bacterial filter to the patient Y piece connection of the patient circuit This will minimise or prevent contamination 23 Signet 615 User Manual For full information about servicing the Signet 615 please refer to the Service Manual 6 1 Service intervals and service components for Signet 615 Item No Product Interval in Months Qty Part No 1 Anti Hypoxic device 12 1 AHD60 99 2 Rotameter 5 Tube 12 1 A5047 99 3 Selectatec Block 12 1 A605 99 4 Regulator Primary 12 3 RG1 99 5 Regulator Secondary 12 2 RO7 99 6 Oxygen Failure Alarm 12 1 A3055 99 7 Ventilator Drive 12 1 A3056 99 8 Manifolds 12 3 A3057 99 9 Patient Block 12 1 A307 99 10 Scavenge Block 12 1 A3027 99 11 Signet 615 Service kit 12 1 A600 99 24 Signet 615 User Manual 7 Specifications 7 1 Physical 7 1 Physical OMS MC E 1515 mm WIA ca ie cncecaas dias cgcesnerveceanccecnsnte 615 mm DG tics ssesice cones seaside cavtenescovsineve 925 mm WISI ss Sererat ies itaadetteasceesctseanes 90 kg not including vaporiser or absorber 7 2 Electromagnetic Compatibility 7 2 1 Electromagnetic Emissions The Signet 615 anaesthetic workstation is suitable for use in the electromagnetic environment specified in the table below The user must ensure that it is used in such an environment
13. air nitrous oxide and oxygen are connected from the wall as well as all pin index reserve cylinders All yokes are pin indexed and once cylinders are located can be secured into position The Signet 615 is fitted with diameter ring indexed gas fittings and colour coded hoses for wall gas supply white for oxygen blue for nitrous oxide and black and white for air N Signet 615 User Manual 2 9 Main regulators The regulator and yoke for each gas are assembled in line to reduce the risk of high pressure leaks The gauge for each gas is connected by a copper tube in parallel The brass yoke bolt RG203 which has the Bodok seal RG204 attached to it and is fitted with a sintered bronze filter RG2031 passes through the yoke assembly and is screwed into the yoke adaptor body RG201 A stainless steel banjo bolt RG206 is used to mount the regulator main body RG201 to the adaptor body RG201 and the use of Dowty Seals RG205 prevent any leaks from occurring A pressure relief valve not shown is fitted to the underside of the regulator body RG101 and is set to start relieving at 600 kPa Note Bodok seals must be examined and replaced if necessary every time the cylinders are replaced 2 10 Second stage regulators There are two second stage regulators fitted one each for the oxygen and nitrous oxide supplies These regulators are situated down stream from the anti hypoxic device and flowmeter assembly They are used
14. al sohygmomanometer can then be used 2 18 1 Accessory power The Signet 615 can be fitted with an optional 4 outlet power board at the top rear of the machine The power board is designed to prevent items other then monitors to be plugged in and is protected by an earth leakage circuit breaker or ELCB On the bottom right hand corner is a fitting for E P Earth If the 4 outlet power board is supplied a short connector cable is used to power some of the rotameter backlighting Second the ventilator power cord may also be connected here leaving the other 3 outlets for the operator s own requirements eg patient monitoring 15 Signet 615 User Manual 3 Preparing for use 3 1 Protocol for checking the Anaesthetic Machine This is one of the College Policy Documents of the Australian and New Zealand College of Anaesthetists The College Policy Documents set down the formal council approved guidelines for practice in a wide range of circumstances Hospitals require these documents to be readily accessible to relevant staff at all times for reference as required The Policy Documents are also referred to by Government and other bodies especially in the process of accreditation of health care facilities Where the Signet 615 is assembled with other components of an anaesthetic system such as ventilators or breathing systems and these components were not supplied by Ulco then the personnel performing the assembly are r
15. alv Esiin nessis ADE switch selects Bain or Lack configuration Paediatric circuit Jackson Rees system Magill CirCuit ceeeeeeeeeeeees For spontaneous breathing anaesthesia Bain adaptor ssssssessssssssessssneenee For controlled breathing anaesthesia Bain circuits essesoneeeeneeneeeene ne Co axial circuits for use with Bain adaptor CO2 ADSOIDET ceeeeeeeeeteeeeeeeeee Optional Capacity 1 or 2 kg capacity Signet 615 User Manual 8 Terms and conditions All merchandise to be returned must have prior written authorisation by Ulco and a valid Return Goods Authorisation RGA number shall appear on the shipping label packing slip purchase order and any other related documents When requesting authorisation to return material the following information should be provided Customer purchase order and date Ulco invoice number and date and method of shipment available form delivery document Part number quantity and description of goods to be returned Reason for returning goods Pon er The following are acceptable reasons for return of goods 1 Material failure within warranty period 2 Service or repairs 3 Ordered in error or duplication of order Any shipping errors or shortages of goods must be reported to Ulco within seven 7 days of receipt of such goods Goods are subject to any terms of any applicable warranty Premature failure of products shall be accepted for return at Ulco s d
16. ard to the information available at the time of their preparation and the practitioner should therefore have regard to any information research or material which may have been published or become available subsequently Whilst the College endeavours to ensure that policy documents are as current as possible at the time of their preparation it takes no responsibility for matters arising from changed circumstances or information or material which may have become available subsequently Promulgated 1984 Reviewed 1990 1996 Date of current document Oct 1997 This document is copyright and cannot be reproduced in whole or in part without prior permission 3 2 Operational checklist procedure pre testing The procedure described below is one method of checking out the Anaesthesia machine that will detect almost any serious problem Special procedures may be required if the machine has been modified or has special medical equipment attached to it The complete check out procedure or its equivalent should be performed prior to the first time a machine is used each day The main checks should also be carried out before each use of a machine on a different patient Ensure that an anaesthetic machine checklist is completed as the procedure is carried out with all details submitted Comprehensive pre use and or daily inspection procedure is a vital component of a complete anaesthesia patient safety program It must not however be relied upo
17. as manifolds ndinoda diandani diadenn danien sadaa dindaa diaii 12 2 9 Maimr eg lators sessen E E A A ANS 13 2 10 Second stage reQulators cccccccceeeeeeeeeeeeeeeeeeeeeeeeeeeeeeseeeeeeeeeeeeeeeeeeees 13 2 11 Pressure gauges x iccscicicsiscweancaineusaunmssedaceceeienensneiessetadsiieuiiesdnberedsedbenenedeveswontade 13 2 12 MEAVENOING sca dacmecsncensscd a A A EA aE 13 2 13 Auxiliary oxygen OUtlet eee eee ceeccceeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeenaeeeeeeeeeeeeeneees 13 2 14 Pipeline hose assemblies cceeceeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeees 13 Signet 615 User Manual 2 157 Patient Circuitry gegen ee ne en er eee eee eee ee 14 ZV TGRC INCI CCU Ns A he Ne Aa AIS Aa et a 14 2 16 Oxygen failure Warning device cece eeeeeeeeeeeceeeeeeeeeeeteeseeeeeeeeeeeeees 14 2 177 Auxiliary Power Outlets 25sec less tose eas sceceretases sevaieacueutyece ayeneeesveaadeesvseneevavedes 14 2 18 Other accessories rats te ses as ete eee ec eet enact ete eee 15 2518 1 AACCESSOFY DOWN cess cessation ois cee ees ds ees ee ee ee 15 Preparing for USC ssc direc eeeecccdccctcedevnshccasctanceseeneeeduenetwciddentseceunasess 16 3 1 Protocol for checking the Anaesthetic Machine ccccccceeceeeeeeeeeeeeeeeees 16 3 2 Operational checklist procedure pre testing cceeeeeeeeeeeeeeeeeeeeeeeeeeees 19 3 2 1 Visual examination Ghee ee Ole hie ie eh ea ah Nie eh Se aah og eh ha 19
18. ber to be swapped from side to side gt Internally mounted mains outlets used to power options 1 6 1 Overall strengths gt sturdy strong durable and easy to understand construction gt high quality and quantity of patient safety features gt pure flexibility of design allowing tailoring of options to exact requirements 1 6 2 Typical configuration gt Signet 615 3 gas 5 Tube machine fitted with anti hypoxic device as standard gt 3 drawers standard gt A internally mounted mains power outlets IEC type N Signet 615 User Manual 1 external mains outlet for use with powered vaporisers IEC type EV500 ventilator OPTIONAL 2kg absorber OPTIONAL Vaporiser s OPTIONAL Auxiliary flowmeter OPTIONAL Writing table Universal arm OPTIONAL Second absorber mounting post OPTIONAL Auxiliary power outlet APB70 OPTIONAL VV VV VV VV WV 1 7 Safety Precautions 1 7 1 Powering the unit up for the first time The unit must be connected to an AC mains supply of 240 V only When power is supplied the power available lamp at the inlet will light All Ulco supplied options such as patient monitors or ventilators will be powered when the main front panel power switch is turned to the ON position The electro luminescent backlight of the medical gas flow meters will only be turned on when the driving gas supply is connected to the air or oxygen ports at the rear of the machine 1 7 2 Follow the Inst
19. ctatec system allows for interchange ability of vaporiser s either for the use of an alternate volatile agent or for maintenance and servicing as well as rendering the machine vapour free if necessary Vaporisers can be easily mounted on the back bar via the Selectatec mounting and should be securely locked into place Vaporisers not attached to the anaesthesia machine must be prevented from tipping over Storage racks are available to store unused vaporisers Vaporisers should be emptied prior to being moved All vaporisers used with the Signet 615 should be compliant with IS08835 4 Note It is important to read the relevant instruction manual issued with each vaporiser prior to use 11 Signet 615 User Manual 2 5 Ventilator The EV500 ventilator can be mounted to the left hand upright of the machine The ventilator mount fits into the bracket All parts can be tightened into position with locking screws The base plate is fitted to the mount and the ventilator is then secured to the base plate with the four nylon screws supplied The ventilator drive hose can then be connected The drive gas connection for the ventilator is the last gas inlet on the right of the gas manifold Air or oxygen drive are optional The ventilator drive gas inlet is supplied with the correct gas hose and ring index for the drive gas specified e g Oxygen Note that the ventilator silencer is connected to the back of the vent
20. dure Check sheets published by the Australian College of Anaesthetists Supplied help by suggesting test procedures If a vaporiser or absorber or circuit is changed it is important not to assume there is no leak In the event of a major leak the bellows of the ventilator will stop rising and start to fall The monitor display will start to flash and the low pressure light will illuminate 15 seconds later an audible alarm will sound which can be silenced by touching the off reset button on the ventilator muting the alarm for 60 seconds Once the leak problem has been solved and there is sufficient difference between the end inspiratory pressure and the end expiratory pressure 6cm H20 or the bellows are refilled the ventilator will cancel all alarms and will begin to cycle normally For further details regarding the EV500 ventilator see the user manual 22 Signet 615 User Manual 5 Care and Cleaning For the workstation to work safely and reliably it must have on going planned maintenance and cleaning Service intervals are described in Section 6 1 The workstation itself requires little cleaning but the actions described in Section 5 1 should be performed at least daily or preferably after each procedure Only those components in direct contact with expired patient gases such as breathing circuits and breathing system components like absorbers ventilator bellows and canisters will require regular disinfection
21. e Mains power quality should be that of a typical commercial or hospital IEC 61000 4 5 1 kV common mode environment Voltage dips lt 5 Urt Mains power quality should be that of short gt 95 dip in Ur a typical commercial or hospital interruptions and for 0 5 cycle environment If the user of the voltage anaesthetic workstation requires variations on 40 Ut continued operation during power power supply 60 dip in Ur mains interruptions it is 25 Signet 615 User Manual input lines for 5 cycles recommended that the anaesthetic workstation be powered from an IEC 61000 4 11 70 Ut uninterruptible power supply or a 30 dip in Ur battery for 25 cycles lt 5 Ur gt 95 dip in Ur for 5 sec Power frequency 3 A m Power frequency magnetic fields 50 60 Hz should be at levels characteristic of a magnetic field typical location in a typical commercial or hospital environment IEC 61000 4 8 Note In the table above Ur is the AC mains voltage prior to application of the test level 7 2 3 Recommended Separation Distance In the following table P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and d is the recommended separation distance in metres m Portable and mobile RF communication equipment should be used no closer to any part of the anaesthetic workstation than the recommended separatio
22. e anaesthetist Gas Delivery System The check shall include 2 1 3 1 Quantifying and minimising leaks 2 1 3 2 Excluding crossed pipelines within the machine 2 1 3 3 Ascertaining the correct functioning of non return valves throughout the system 2 1 3 4 Ascertaining the integrity of oxygen failure prevention and warning devices Anaesthetic Vapour Delivery System The check shall include the accuracy of vapour output and delivery devices It is essential to ascertain that the machine as supplied complies with the relevant Australian or New Zealand standard The check specified above must be undertaken by a suitably qualified person usually the service provider The check must be recorded with inclusion of information as to what was checked and by whom After servicing the particular checklist will relate to the actual service performed Level Two check This check must be undertaken by a suitably qualified person Such as an anaesthetist technician or nurse in accordance with a protocol specific for the particular machine Thus several different protocols may be required in a single hospital These will serve to verify the correct functioning of the anaesthesia machine before it is used for patient care Equipment required for the tests must be available on each machine 2 2 1 2 2 2 High Pressure System 2 2 1 1 Check oxygen cylinder supply Ensure that cylinder content is sufficient for its intended purpose 2 2 1 2 Check
23. e of flow is indicated by the top edge of the float bobbin against the flowmeter scale Indicated flows are accurate to within 1 875 of indicated flow 0 625 of the full scale Therefore for a flowmeter with a full scale reading of 10 L min set to deliver 7 5 L min the maximum permissible error is 7 5x1 875 10 0x0 625 100 0 141 0 063 L min 0 204 L min L min Gases passing through the flowmeter mix together at rates of flow selected by the anaesthetist Passing along the back bar part of the combined gases enter the vaporiser inlet if selected If the vaporiser is fitted and is in the OFF position the gases bypass the vaporising chamber and pass directly to the common gas outlet via the non return valve fitted in the terminating block of the back bar From here they pass to the anaesthetic equipment and to the patient If the vaporiser is selected ON gas mixtures entering the vaporiser collect a proportion of the anaesthetic agent from the vaporising chamber within The percentage volume is determined by setting the vaporiser control at the percentage figure calculated by the anaesthetist Having passed through the vaporiser the gas mixture now combined with the anaesthetic agent again enters the back bar and is delivered to the patient as described previously See the vaporiser manual for further details 2 3 Patient Block The patient block is mounted on the side rail of the working area In its entir
24. em check its integrity and the functioning of unidirectional valves This can be accomplished with a breathing bag on the patient limb of the Y piece Ventilate the system manually using an appropriate fresh gas flow Observe inflation and deflation of the attached breathing bag and check for normal system resistance and compliance Observe movement of unidirectional valves Check function of adjustable pressure limiting APL valve by ensuring easy gas spill through APL when the two breathing bags are squeezed 2 2 3 Automatic Ventilation System This should be checked according to the manufacturer s recommendations This test protocol must be present on the machine A test lung Such as a suitably compliant bag may be used to check the function of the ventilator Where practicable gas flow should be reduced to check for leaks The functioning of disconnection and high pressure alarms should be checked at this time 2 2 4 Scavenging System This should be checked after connection to APL valve and ensuring a free gas flow If there is negative pressure in any part of the system ensure that this does not lead to emptying of the breathing system With the patient occluded a full breathing system should not empty with the APL valve open 2 2 5 Emergency Ventilation System Verify the presence and functioning of an alternative method of providing oxygen and of controlled ventilation such as self inflating bag 2 2 6 Other apparatus to be used This
25. esponsible for providing a checklist for the anaesthetic system The College Policy Document Protocol for checking the Anaesthetic Machine reads as follows 1 Introduction 1 1 The regulated supply of gases and vapours for anaesthesia and the provision of controlled ventilation for the patient are the main functions of the anaesthetic machine or workstation Because oxygenation and ventilation are essential for every patient and because even a brief failure to maintain them may cause irreparable harm every machine must be regularly and thoroughly checked to ensure that all functions are correctly maintained 1 2 There must be a reserve facility to maintain oxygenation and ventilation of a patient should failure of the primary systems occur 1 3 To ensure early detection of any failure in the anaesthetic machine it is essential that appropriate alarms are present in the machine and that there is monitoring of the state of the patient as specified in IEC 60601 2 13 and Section 1 7 7 of this document 1 4 This protocol incorporates three components 1 4 1 Level one check This is very detailed and is required a on any new machine and b on all machines after the required regular servicing This check will usually be performed by the service person whether from the equipment provider or from the Bio Engineering Department 1 4 2 Level Two check This should be performed at the start of each anaesthetic session 1 4 3 Level Three check T
26. ety it houses the common gas outlet the emergency oxygen flush and a patient safety relief valve set to relieve at 50cm H20 pressure which can be set higher or lower The common gas outlet is a 22 15mm male stainless steel cone with a weight bearing thread for attaching items such as the fresh gas connecting hose to the CO2 absorber or a Bain adaptor The patient block can slide along the side rail to the most convenient position where it can be locked into position Fresh gas from the back bar is supplied to the patient block via the one way valve direct to the back of the common gas outlet This is in turn connected to the patient safety valve housing a safety valve that is adjusted to relieve at 50cm H20 pressure The emergency oxygen flush is supplied with oxygen direct from the oxygen manifold in the console When depressed the oxygen flush flow is set by a metered orifice that leads from the high pressure oxygen side of the flush valve to the common gas outlet The flow is normally 35 to 75 L min 2 4 Vaporisers Various methods of mounting vaporisers are currently used such as the off line or fixed systems The most common is the Selectatec type mounting system in which a mounting block is permanently attached to the back bar and the vaporiser is locked on by means of DZUS aircraft type quick release fastener Gas flow is diverted through the vaporiser via the ports when the Vaporiser is placed on the mounting block The Sele
27. ety valve for leaks by blocking the common gas outlet Raise the pressure in the back bar using the oxygen flow control valve on the flowmeter until the patient safety valve pressure is obtained Check for leaks from the outlet back to the flowmeter a soapy solution can be used to test this w Turn off all gas supplies clean all traces of soap solution if used from the machine 3 2 5 General Assuming all hose connections have been established oxygen flow should first be established at the rotameter Bellows volume is then adjusted on the ventilator see user manual for EV500 ventilator for further details making sure the absorber is on and operational The ventilator can then be turned on and set for the patient The patient is then being ventilated The first line of safety to the patient is the anti hypoxic device Once the nitrous oxide control is fully opened only the oxygen control needs to be used The anti hypoxic device ensures that a nominal ratio of at least one part oxygen to three parts nitrous oxide is delivered at all times should nitrous oxide be used The anaesthetist can choose to increase the amount of oxygen delivered or reduce the amount of nitrous oxide however the 1 3 ratio cannot be breached Air is available at all times with or without the presence of oxygen nitrous oxide or both Should pipeline supply fail the operator simply needs to turn on the supply from the appropriate compressed gas cylinder The cyl
28. he ventilator will continue to operate Once the pressure drops to approximately 225kPa an audible alarm will sound and the nitrous oxide supply through the rotameter will be cut off At the same time the supply of oxygen to the ventilator will cease ensuring all oxygen is available for the patient The flow of oxygen can still be seen at the rotameter At 220kPa there is only about 3 litres of oxygen left in the reservoir cylinder giving some time for the operator to rectify the pressure problems This can be achieved by turning on the reserve cylinders amongst other alternatives Once normal pressure is re established the alarms turn off nitrous oxide will start to flow and the ventilator will start to cycle again The Visiwink only turns red below 125kPa At this stage if oxygen is not being supplied an alternative supply source should be established If air is connected there is a safe reserve with a content of around 21 oxygen 2 17 Auxiliary Power Outlets The Signet mains power supply is switched by the main front panel on off switch and is then distributed to 5 IEC outlets mounted internally in the rear of the machine One of the outlets is used to power the electro luminescent backlight for the flow tubes one supplies power to the external auxiliary outlet for use in powering vaporisers and the other 3 are available to power additional options such as monitors and ventilators These outlets can only be accessed by removing the rear cover
29. his should be performed immediately before commencing each subsequent anaesthetic 1 5 Accreditation for checking the anaesthetic machine requires 1 5 1 Level One Attendance at a manufacturer s course or a programme developed by the hospital s Anaesthesia Department in consultation with a qualified Biomedical Engineer 1 5 2 Levels Two and Three Checks must follow protocols specifically developed for the machine under test All personnel must be trained in correct procedures and accredited to perform them by the Anaesthesia Department The specific protocols should be attached to the machine 2 Protocols 2 1 Level One check This must be performed by on anaesthesia machines a before they enter service and b following all service inspections which must be performed at regular and specified intervals 2 1 1 The Hospital Anaesthesia Department or body responsible for the equipment shall keep a detailed record of the equipment and the checking procedures This process requires that a checklist be 16 Signet 615 User Manual 2 2 2 1 2 2 1 3 2 1 4 2 1 5 2 1 6 maintained The checklist will be based on manufacturer s recommendations The protocols shall describe checking and calibration protocols and the intervals at which these must be performed The anaesthetic machine must have a prominent label to advise of past service s and to indicate when the next check is due This label must be visible to th
30. hould be obtained from Advena Ltd PO Box 30 Leominster HR6 OZQ UK Telephone 44 0 1568 620080 Fax 44 0 1568 620078
31. ilator and that the 30mm male scavenging outlet is on the top of the exhaust Further information regarding the operation of the EV500 ventilator can be found in its user manual 2 6 Soda lime absorber The soda lime absorber mount bracket attaches to the post towards the front of the machine The absorber mount sits over the upright and should be allowed to seat itself into position The top locking screw and side locking screw can then be fastened to hold in position The exhaust hose can then be attached to the 30mm exhaust valve scavenging outlet The absorber fresh gas hose from the common gas outlet can now be connected to the fresh gas inlet on the side of the absorber This connection hose is made from strong reinforced hose so it will not perish No latex tubing is used in Ulco machines Further information regarding the operation of the absorber can be found in its User Manual 2 7 The anti hypoxic device The Signet 615 contains many features to ensure patient well being The first of these is the anti hypoxic device This is a now mandatory device in Australia and many overseas markets This allows the anaesthetist to deliver 100 oxygen to the patient but never less than nominal 25 oxygen in the presence of nitrous oxide in the mix This also means that no nitrous oxide can flow without oxygen Other devices sometimes allow oxygen flow once nitrous oxide has been turned on No Ulco machines allow this meaning that oxygen flow must be e
32. inder pressure gauge on the front of the machine will then register a reading The normal gas pressure range for the Signet 615 is 300 to 550 kPa 20 Signet 615 User Manual 4 Operation 4 1 Medical Gas Mixing Flow meters rotameters for O2 AIR and N20 are used to control the fresh gas flow to the breathing system Turning the flow control knob counter clockwise opens the flow to the flowmeter tube the set flow rate being indicated by the float or bobbin The correct flow rate is read by observing position of the upper surface of the float with respect to the engraved scale on the flow tube WARNING Always check that the float rotates freely during use This proves that the float is free within the tube Should the O2 supply be interrupted all other gases are cut off The O2 Flush push button activates an O2flow of 35 75 L min directly to the common gas outlet This is also useful for initial filling of ventilator bellows and patient breathing systems and is always available Vaporizers can be mounted to the machine backbar When vaporizers are fitted with safety interlock systems only one vaporizer at a time can be selected to ON Fresh gas is delivered from the Common Gas Outlet fitted to the patient block The outlet has a 22 15mm male stainless steel cone with a weight bearing thread for attaching items such as the fresh gas connecting hose to the outlet 4 1 1 Accuracy and the Effects of Bac
33. iscretion and only during the warranty period Goods to be returned which are not under warranty should have been purchased within thirty days of request for return and returned within thirty days after request Goods shall be returned unused and in Ulco containers Goods may be subject to a 20 restocking charge with the exception of goods failure within the warranty period or due to Ulco error The following merchandise is not eligible for return unless proven defective Sterile material unless shipped in error by Ulco Rubber and plastic components that have been used Specially ordered or produced items Goods that have been altered or abused PONE All items to be returned shall be shipped including RGA number to Ulco Medical 25 Sloane St Marrickville NSW 2204 Australia In the European Community returned goods authorities should be obtained from Advena Ltd PO Box 30 Leominster HR6 OZQ UK Telephone 44 0 1568 620080 Fax 44 0 1568 620078 29 GOODS RETURN AUTHORISATION RGA Number Customer Details Name Address State Country Postcode Returned Product Date of Purchase Date of return Reason for returning goods please give a short description of the fault Signature ULCO Medical 25 Sloane St Marrickville NSW 2204 Australia In the European Community returned goods authorities s
34. kpressure The glass tubes are antistatic and electrically conductive and are manufactured to an accuracy of CLASS 2 5 VDI VDE 3513 so that the total tolerance at any given point on the scale is 1 85 of Indicated Flow 0 625 of Full Scale Reading with a ceiling value of 10 Indicated Flow whichever is lower Backpressure may depress the float so that the indicated flow is less than the actual flow For all normal usage it can be safely assumed that the maximum error in indicated flow will not exceed 10 4 2 Circle Systems The Signet should be used in conjunction with Ulco s AB800 soda lime absorber when used as part of a circle rebreathing system 1 When the absorber is in use ensure that the INSPIRATORY and EXPIRATORY one way VALVES can be seen operating and check colour change of the CO2 absorbent 2 For the Switchable version of the absorber check that the bypass lever is set to the desired position i e OFF allows the gas to by pass the soda lime canisters 4 3 Troubleshooting The problem of leaks anywhere in the patient circuit can be difficult to solve and can occur anywhere from the rotameter block forward to the patient circuit This includes gt vaporiser mounts vaporisers themselves how the vaporisers are mounted the common gas outlet connection VV V WV the absorber 21 Signet 615 User Manual gt the patient circuit itself It is important to go through a logical test proce
35. n distance calculated from the equation appropriate for the frequency of the transmitter Field strengths from fixed RF transmitters as determined by an electromagnetic site survey should be less than the compliance level in each frequency range over the frequency range 150 kHz to 80 M Hz field strengths should be less than 3 V m Interference may occur in the vicinity of equipment marked with this symbol o A Immunity test IEC 60601 test level Compliance level Electromagnetic environment guidance Conducted RF 3 Vrms 3 Vrms Recommended separation distance IEC 61000 4 6 150 kHz to 80 MHz d 1 2VP Radiated RF 3 V m 3 V m Recommended separation distance IEC 61000 4 3 80 MHz to 2 5 GHz 80 MHz to 800 MHz d 1 2VP 800 MHz to 2 5 GHz d 2 3VP Notes e At80 MHz and 800 MHz the higher frequency range applies e These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and and mobile radios amateur radio AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the anaesthetic workstation is used
36. n to prevent all equipment related complications Some types of failures may not be detected without an exhaustive inspection protocol and some equipment failures will inevitably occur during use There is no substitute for the continuous presence vigilance and good judgement of a trained anaesthetist during anaesthesia and mechanical ventilation Before starting be sure to have all necessary equipment Start by verifying that the items necessary for the procedure are present Appropriate emergency drugs and equipment should be close at hand Be sure to check Laryngoscopes as they are the equipment items that fail most frequently 3 2 1 Visual examination Visually examine the anaesthesia machine to identify obvious problems such as broken flowmeter tubes or missing probes and breathing circuit connectors Identify and log the machine serial number on the anaesthetic record as this may be needed if a problem were to be suspected Visually check gt Patient pressure gauge shows zero pressure Frame and castors Monitor shelf if fitted Console Working table VV VV WV Drawer for easy movement 19 Signet 615 User Manual 3 2 2 General preparation pre check 1 Turn on the monitoring equipment and allow time to stabilise before calibrating 2 Connect the scavenging system all fittings should be sequential to prevent misconnection Activate the system prior to carrying out any procedure and check to avoid
37. nditions 1 Ulco or its authorised agents must be promptly notified in writing upon detection of the defective material or equipment Defective material or equipment must be returned shipping prepaid to Ulco or its authorised agent Examination by Ulco or its authorised agent must confirm that the defect is in fact covered by the terms of this warranty A Notification in writing of defective material or equipment must be receive by Ulco or its agent no later than two 2 weeks following expiration of this warranty In order to assume complete protection under this warranty the warranty registration card and or periodic manufacturer s service record if applicable must be returned to Ulco within 2 weeks of receipt of the equipment The above is the sole warranty provided by Ulco No other warranty expressed or implied is intended Representatives or agents of Ulco are not authorised to modify or amend the terms and conditions of this warranty 1 2 About this manual This manual provides information for the preparation assembly and care of the Signet 615 anaesthesia machine together with suitable equipment from the Ulco range Although this equipment has been carefully designed for simplicity of assembly and use it is recommended that the contents of this manual be studied before attempting preparation or care of the equipment Explanatory diagrams are provided in order to help the reader understand the concepts described This
38. o These agreements are available from Ulco Technical Services 1 7 5 Use of anaesthetic agents Explosive anaesthetic agents such as ether or cyclopropane must not be used due to the risk of fire Ulco accepts no liability if the wrong anaesthetic agent is used 1 7 6 Power Connection Ulco equipment is to be used only in rooms with mains power supply installations complying with national safety standards Signet 615 User Manual Electrical connections for other equipment not listed here should only be made following consultations with the respective manufacturers or other expert For full details of the electrical environment in which the Signet may be used see Section 7 2 of this document 1 7 7 Monitoring and alarms If the unit alarms check the patient Establish that the patient is being ventilated correctly This unit must be used in conjunction with equipment providing the following alarms and monitoring capabilities e Inspiratory oxygen concentration Anaesthetic agent concentration Airway pressure CO2 concentration Exhaled volume Breathing system integrity Continuing pressure These will help ensure patient safety make precise ventilation possible and so achieve the best possible ventilator parameters for the patient Signet 615 User Manual 2 Major components of the machine Pipeline Cylinder Patient Pressure Pressure Pressure Main Gauges Gauges Gauge On Off Switch
39. polluting the Operating Room 3 Check back bar integrity and Selectatec type mounts see figure A3046 Clear all obstructions such as tubes and lines which could prevent correct Vaporiser mounting 4 The seal between the vaporiser and the Selectatec mounting block is dependent on an O ring retained at the bottom of each of the valve stems It is therefore important that they be examined each time the vaporiser is removed from the anaesthesia machine Note Make sure that only one O ring be kept with each machine Vaporisers not attached to the anaesthesia machine must be prevented from tipping over and should be emptied prior to being moved 3 2 3 Cylinder Fitting Check the cylinder for correct gas type Check that an intact Bodok seal is fitted to the yoke Remove the seal wrap from the cylinder valve Open the cylinder valve momentarily to blow any foreign matter from the gas outlet a e NNP Insert the cylinder into the apparatus yoke ensuring that the outlet orifice of the cylinder valve engages with the inlet of the yoke Tighten the yoke clamping screw 3 2 4 Component integrity The apparatus is now ready for testing prior to use All the components and assembly are fully tested prior to despatch from our works but may have loosened during transport The following ensures components are secure Fit the gas cylinders or pipeline supply as detailed above Test the vaporiser spacer cone socket joints and saf
40. power not listed above the recommended separation distance d in metres m can be estimated using the equation applicable to the frequency of the transmitter where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer 7 3 Symbols These symbols appear on the workstation and its associated equipment Symbols Refer to accompanying Protective Earth Type CF Applied documents Part Equipotential Alternating Date of Grounding Ne Current Manufacture Power Off Power On aad Manufacturer pneumatic and pneumatic and electrical electrical 27 Signet 615 User Manual 7 4 Standard items GAS CirCUjtS aisis Pipeline oxygen and nitrous oxide 400 kPa with air gauge as an option Back bar assembly 06 All back bar components Selectatec Type FIOWIM GUGM ies fs scscccctecsesetsacscccceaes 3 gas oxygen nitrous oxide and air Vaporiser MOUNTS Selectatec type x 2 Oxygen failure eseese Warning device with audio visual warnings Drawer UNIUS s issssssirseisssss 3 Common Gas outlet Emergency O2 flush 08 gt 35 L min flow Patient safety valve ssassn 50 cm H20 Male CONnNeCto ceeeeeeees 22 15 mm 7 5 Optional Items Vaporisers ccccceceeeeeeesssseees Any agent Selectatec type Absorber Bellows cccceeee Combined unit Anti hypoxic device seses Standard equipment maintains 21 O2 flow MCS v
41. r can be sealed by using a bung supplied The wall vacuum tubing is then connected to the connector on the back of the block The flow meter tube has a filter silencer fitted this may require replacement after constant use as the filter can become blocked 2 13 Auxiliary oxygen outlet An auxiliary oxygen outlet is mounted on the right hand frame upright where an oxygen flowmeter can be used This oxygen flow meter can be used to deliver oxygen to the patient instead of using the rotameters and standard common gas outlet This is used for example with neurolipse relative analgesia and local anaesthesia safely bypassing the possibility of accidental vaporiser delivery or in circuit complications The O 15 L min flowmeter can then be connected to the auxiliary outlet It should be tested to make sure it is operating correctly 2 14 Pipeline hose assemblies The pipeline hose assemblies are fitted with non interchangeable connectors handwheels at both ends of the hose They are suitable for Australian wall outlets or cylinder regulators Each type of gas hose and handwheel is 13 Signet 615 User Manual colour coded and diameter size indexed to the ISO International Standards Organisation standard for that particular gas Each hose must be connected to the correct gas inlet and sufficiently tightened to prevent gas leaks The anaesthesia machine is provided with hooks at the top rear of each leg for hanging the hoses 2
42. ructions for Use In order to use the equipment these instructions must be fully read and understood and strictly followed Any equipment mentioned is only to be used for the intended purpose 1 7 3 Liability for proper function or damage This equipment is an adjunct to patient safety and it must in no way replace the normal monitoring by skilled personnel The manufacturers accept no responsibility for incidents arising from either incorrect use or malfunction of this equipment If the equipment is serviced or repaired by persons not employed or authorised by Ulco or if the equipment is not used for the purposes for which it is intended then the liability for the proper function of the equipment is transferred to the owner operator Where the Signet 615 is assembled with other components of an anaesthetic system such as ventilators or breathing systems and Ulco did not supply these components then the personnel performing the assembly are responsible for providing a checklist for the anaesthetic system 1 7 4 Maintenance and Repairs An authorised Ulco Technical Service Representative must perform maintenance of this equipment Ulco products in need of factory repairs must be sent to the nearest local agent or direct to Ulco Ulco recommends that anaesthesia products equipment be serviced at intervals stated in Section 6 1 of this manual Periodic Manufacturer s Service Contracts are available for products manufactured and or sold by Ulc
43. stablished first before nitrous oxide flow is able to flow The device has been designed to eliminate inherent faults common in other similar products In some such devices both the oxygen and nitrous oxide begin to flow as soon as the nitrous oxide control is turned on The operator can thus become accustomed to setting all flows whilst only using the nitrous oxide flow control This is a safe practise assuming the anaesthesia machine is fitted with an anti hypoxic device Many machines both in Australia and overseas however do not have such a device enabling the operator to deliver a 100 nitrous oxide flow inadvertently The Ulco anti hypoxic device prevents this by ensuring that no nitrous oxide is permitted to flow unless the oxygen flow control is first turned on The nitrous oxide needle valve is held in place by the oxygen flow control The nitrous oxide flow control knob is free to rotate however in order to prevent damage if force is applied trying to achieve a flow when no flow is allowed When correctly adjusted and calibrated the device will prevent the delivery of hypoxic mixtures and oxygen flow will be maintained at 25 nominal flow 5 The device itself is tamper proof and cannot be interfered with by the operator but is easy to adjust and calibrate by trained technical staff 3 Gas manifold The gas manifold is fitted to the rear of the machine All gases that supply the machine are connected via the manifold Pipeline
44. that piped gas supplies where present are at the specified pressures and that following high pressure system checks the cylinders are turned off 2 2 1 3 Confirm correct pipeline supply by using an oxygen analyser or multigas analyser distal to the common gas outlet Low Pressure System 2 2 2 1 Check control valves and flow meters Turn on each gas and observe the appropriate operation of the corresponding flow meter Check the functioning of any interactive anti hypoxic device 2 2 2 2 Check that any required vaporiser is present 2 2 2 2 1 Check that adequate anaesthetic liquid is present 2 2 2 2 2 Ensure that the vaporiser filling ports are closed 2 2 2 2 3 Check correct seating and locking of a detachable vaporiser 2 2 2 2 4 Test for circuit leaks for each vaporiser in both on and off positions 2 2 2 2 5 Ensure power is available for electrically operated vaporisers 17 Signet 615 User Manual 2 2 2 3 Check for pre circuit leaks using a method sensitive to 100mL minute and appropriate for specific machine 2 2 2 4 Breathing systems Check the general status to ensure correct assembly and absence of leaks The precise protocol will depend on the anaesthesia circuit to be used 2 2 2 4 1 Perform leak test on the breathing system by occluding the patient connection applying a fresh gas flow of 300mL min and ensuring that a pressure of greater than 30cm H20 is sustained 2 2 2 4 2 In the circle syst
45. to calibrate and fine tune the anti hypoxic device See separate instructions The second stage regulators are also used as a buffer to protect the anti hypoxic device against any pressure fluctuations that may occur in both the pipeline and the cylinder regulated pressure Pipeline pressure ccceeeeeeeeeeeeeeeeeeteeeees 415 kPa Cylinder regulated pressure ss cc 350 370 kPa Second stage regulator pressures when set to deliver the correct mixtures on the anti hypoxic device are usually lt 220 kPa This allows for fluctuations in supply pressure of more than 100 kPa before the set flows are affected 2 11 Pressure gauges Pressure gauges are well placed at eye level for ease of viewing The left 3 show pipeline pressure while the right 3 show the pressure in the reserve gas cylinders A simple visible indicator called the Visiwink is mounted below the ON OFF control When green it indicates oxygen is ON When red it indicates that oxygen pressure is OFF 2 12 Scavenging On the left hand upright of the frame is the scavenging block which should be connected to wall suction Adequate scavenging can be achieved by adjusting the ball to the marked line Vacuum adjustment is via the control at the front The vacuum reservoir for scavenging is integrated into the frame of the machine using both the frame upright The scavenging block has two locations for pink red scavenging tubing to be connected If only one is being used the othe
46. uction of the frames provides a stable and unobstructed unit for the mounting of a wide range of anaesthesia equipment accessories The Signet 615 can be easily upgraded from its basic configuration with optional accessories and attachments including a full range of patient monitors to provide a comprehensive anaesthesia workstation If equipment that has not been specifically designed or supplied by Ulco is to be attached to the Ulco machine it is recommended that customers consult Ulco as to the suitability of the equipment and necessary modifications to the apparatus Ulco and its agents provide a comprehensive regular maintenance service and it is recommended that advantage be taken for the safe and reliable upkeep of this equipment Refer to the accompanying service manual for details on how to maintain your Ulco machine There is a service contract included with the equipment please fill it in and return it to Ulco Customers requiring further service or advice with operating problems should contact Ulco or one of their accredited agents 1 6 Major features gt All working surfaces are designed to be easy to clean and front wheels are lockable to prevent unwanted movement v A monitor shelf is available as an option v An aluminium accessory rail is fitted to the sides of the working area for easy attachment of many options gt The absorber post can be mounted either on the left or right hand sides or both allowing the absor
47. user manual should be read in conjunction with the user manual s for the vaporisers ventilator and absorbers 1 3 Intended Use The Signet 615 Anaesthesia Machine is an apparatus for providing continuous gas inhalation anaesthesia for human adults and children above 5kg body weight The apparatus is intended for used solely in an operating or induction room The apparatus is intended to be use with hospital gas supply pressures within the range 300 500 kPa The apparatus is intended to be use under the continuous control of a person suitably trained and clinically qualified in its use ep Signet 615 User Manual To comply with the Anaesthetic workstation station standard IEC 60601 2 13 the Signet 615 must be used with adequate monitoring and alarms The stated monitors and alarms can be found in Section 1 7 7 of this manual 1 4 Device Classification The Signet 615 Anaesthesia Machine is classified as follows e Class equipment for the purposes of electrical safety e Type CF applied part e Continuous Operation 1 5 Background Anaesthesia machines such as the Signet 615 are engineered to very high standards of design and finish and all units are able to accommodate the most comprehensive specifications required in modern anaesthesia Ulco machines are manufactured from non magnetic materials such as stainless steel anodised aluminium and chromed brass or acetal with moulded covers made from Kydex The constr
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